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CompletedNCT05113147Updated Nov 9, 2021

Disruptive Behavior in the Operating Room

An observational study in Disruptive Behavior, sponsored by Pontificia Universidad Catolica de Chile. Completed at 1 site in Chile. Per ClinicalTrials.gov, last updated 2021-11-09.

Sponsored by Pontificia Universidad Catolica de Chile · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
20
Sex
All
01

Study summary

Background: The operating room (OR) environment presents specific conditions that put stress on work dynamics. Disruptive behavior (DB) among members of the health team is recognized to affect work dynamics and patient outcomes. The objective was to explore the perceptions of different members of the health team, including surgeons, about the occurrence of DB and the work dynamics in the OR.

Study design: Qualitative exploratory study, based on semi structured individual interviews. Twenty participants were sampled until data saturation, including surgeons, anesthetists, nurses among other. Data extraction from verbatim transcriptions was performed by investigators via qualitative analysis software, using grounded theory framework.

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METHODS

A qualitative exploratory study was carried out within an analytical and relational framework of the contents [19,20]. The study was approved by a Scientific Ethics Committee (project ID: 15-340) and meets the quality standards for reporting qualitative Research (COREQ checklist).

Selection of participants Intentional theoretical sampling was performed, which considered the representation of different members of the health team to seek maximum heterogeneity.

The inclusion criterion was that the health members had at least one year of experience in the operating room. Participants were included until achieving data saturation from the information obtained.

Data collection In-depth individual interviews were based on a semistructured script designed to investigate the perceptions of the participants about the activity they performed, the ideal working conditions, the presence of disruptive behaviors, and their management. The final version of the script was reached after the first four interviews. Once the adjustments were made, the same script was used with the other participants.

The interviews were conducted by two interviewers (DZ and MC) with experience in this collection technique and who were not linked to the activities of the health team that was the subject of this study. The information was collected in 2017 and 2018. The participants were invited by email, and once they signed an informed consent, which explained the research´s goal and information about their participation. Once they agreed to participate, the interviewers interviewed an office face-to-face to guarantee privacy and confidentiality. Interviews lasted an average of 45 minutes, and all were audio-recorded and later transcribed verbatim.

Data analysis The participants' responses were analyzed with open and axial coding, based on the grounded theory model to relate the categories emerging from the responses.

Grounded theory is based on the analysis of the narrative contained in the interviews. This in turn leads to the development of codes, categories and themes based on the descriptions to culminate in hypotheses of how these themes interact. Atlas.ti v8.0 software was used for the data analysis (ATLAS.ti Scientific Software Development GmbH, Lietzenburger Str. 75, D-10719 Berlin, Germany).

Six researchers from the team collaborated in the analysis of the transcripts through an iterative process of intersubjective data triangulation sessions until definitive categories and guiding questions were reached regarding the phenomenon under study.

After the analysis, all participants received an email, who explained the findings and asked for feedback (member checking).

02

Conditions studied

  • Disruptive Behavior

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Keywords

  • Disruptive Behavior
  • Patient Safety
  • Operating Room
  • Surgeons
  • Effective Teamwork
  • Organizational Culture
  • Qualitative Study
03

In context

Problem Behavior

517 studies on the registry are indexed under Problem Behavior; 92 are open to participants now.

This study's enrollment of 20 is below the median of 208 across 119 observational studies indexed under Problem Behavior.

Browse Problem Behavior studies →

Lead sponsor

Pontificia Universidad Catolica de Chile is the lead sponsor of 215 studies on the registry; 56 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Twenty participants included (surgeons n = 12, anesthetists n = 2, residents n = 2, nurses n = 2, technicians n = 2).

Inclusion criteria

  • Health members working in the operating room.

Exclusion criteria

Exclusion Criteria:

  • Less than one year of experience in the operating room.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
20 participants (actual)
Patient registry
No

Interventions

  • OtherIn-depth individual interviews

    In-depth individual interviews were based on a semistructured script designed to investigate the perceptions of the participants about the activity they performed, the ideal working conditions, the presence of disruptive behaviors, and their management.

06

What researchers measure

Primary outcomes

  1. Perceptions about the occurrence of disruptive behaviors and the work dynamics in the operating room

    In-depth individual interviews were based on a semistructured script designed to investigate the perceptions of the participants about the activity they performed, the ideal working conditions, the presence of disruptive behaviors, and their management

    Time frame: Up to 45 minutes

07

Study locations

1 site
  • María-Jesús Lira
    Santiago, Santiago Metropolitan 8330077, Chile
08

References and documents

Individual participant data

Plan to share: No — To protect the confidentiality of the participants, interview transcripts will not be shared.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05113147
Lead sponsor
Pontificia Universidad Catolica de Chile
Responsible party
Maria Jesus Lira (Nurse, Pontificia Universidad Catolica de Chile) — Principal investigator
First posted
Nov 9, 2021
Start date
Mar 20, 2018
Primary completion
Mar 20, 2018
Completion
May 30, 2018
Last update
Nov 9, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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